2种新的中国人β-地中海贫血基因突变类型CD13/14(-C)和beta nt1582(A>G)突变  

Two Novel β-thalassemia Gene Mutations Were Detected in Chinese Patients:CD13/14(-C) and beta nt1582(A>G),PolyA(AATAAA>GATAAA)

作　　者：潘小英[1] 唐斌[2] 梁驹卿[1] 郜红艺[3] 尹爱华[1] 吴菁[1] 王继成[1] 钟燕芳[1] 朱伟杰[2] 

机构地区：[1]广东省妇幼保健院暨广州医学院附属广东省妇儿医院产前诊断中心,广州510010 [2]暨南大学生命科技学院,生殖免疫研究所,广州510632 [3]广东省妇幼保健院暨广州医学院附属广东省妇儿医院病理科,广州510010

出　　处：《生殖与避孕》2009年第7期438-442,共5页Reproduction and Contraception

基　　金：国家科技部"十五"科技攻关项目(2002BA709B10);"十一五"科技攻关项目(2006BA10508)的部分工作

摘　　要：目的:报道2种新的中国人β-地中海贫血(β-thalassemias,β-地贫)基因突变类型CD13/14(-C)和beta nt1582(A>G)突变。方法:疑似β-地贫患者10例,其中7例为临床疑似轻型β-地贫基因携带者,1例为临床疑似重型β-地贫患者,2例为父母双方均为β-地贫基因携带者的胎儿。应用聚合酶链反应联合反向点杂交技术(PCR-RDB),以及基于PCR技术的DNA测序技术检测β血红蛋白基因。根据患者表型和以往文献报道,对新发现的基因突变性质进行分析。结果:检测出2种β-地贫常见基因突变型,分别是IVS-2-654(C>T)和-28(A>G)。检测出5种β-地贫稀有基因突变型,分别是beta nt1582(A>G),PolyA(AATAAA>GATAAA);CD13/14(-C);beta nt1586(A>G),PolyA(AATAAA>AATAGA);IVS-1-1(G>T);IVS-2-2(-T);其中前2种为新发现的β-地贫基因突变类型。结论:发现了2种新的β-地贫基因突变类型,其表型效果可能为β0或β+。对常规基因检测技术不能诊断的β-地贫疑似病例,可作DNA测序进行确诊。Objective： To identify two novel β-thalassemia gene mutations in Chinese patients： CD13/14 （-C） and beta nt1582 （A〉G）, PolyA （AATAAA〉GATAAA）. Methods： Ten suspected cases were selected in the prenatal diagnosis center for further diagnosing β-thalassemia. Among them, 7 cases were suspected as β-thalassemia trait, 1 case was suspected as β-thalassemia major, and 2 cases were fetus whose parents were β-halassemia gene carriers. The samples were determined by using polymerase chain reaction and reverse dot blot hybridization （PCR-RDB） techniques, and β-hemoglobin direct genomic sequencing （DGS）. Results： Two types of common β-thalassemia gene mutations were detected with PCR-RDB in 3 patients and 1 fetus, which were IVS-2-654 （C〉T） and -28 （A〉G）. Five types of rare β-thalassemia gene mutations were detected with DGS in 6 patients and 1 fetus. Among these 5 rare gene mutations, 2 novel gene mutations had been found, which were beta nt 1582 （A〉G）, PolyA（AATAAA〉GATAAA） and CD 13/14（-C）. Conclusion： Two novel β-thalassemia gene muta- tions were detected, which phenotype would be β＋ or β. If a suspected case couldn＇t be identitied by PCR-RDB, DNA sequencing should be used for further investigation.

关 键 词：Β-地中海贫血 DNA测序 产前诊断 稀有基因突变 

分 类 号：R556.61[医药卫生—血液循环系统疾病]